WT1 inhibitors belong to a class of chemical compounds that have garnered significant attention within the realm of molecular biology and drug discovery. These inhibitors target a specific protein known as WT1, which plays a critical role in cellular processes. The abbreviation WT1 stands for Wilms' tumor protein 1, and it is a transcription factor that serves as a pivotal regulator in various developmental stages and normal cellular functions. The primary objective of WT1 inhibitors is to modulate the activity of this protein, thereby influencing downstream gene expression and molecular pathways. Structurally, WT1 inhibitors are designed to interact with the active site of the WT1 protein, hindering its ability to bind to DNA and regulate gene transcription. This interaction is vital for controlling the expression of numerous genes involved in cellular differentiation, proliferation, and apoptosis. By modulating the function of WT1, these inhibitors can impact various cellular processes and pathways that rely on WT1-mediated gene expression.
Researchers have meticulously engineered a diverse array of WT1 inhibitors with varying chemical structures to optimize their binding affinity and selectivity for the WT1 protein. The development of WT1 inhibitors is rooted in the recognition of WT1's essential role in cellular homeostasis and development. Understanding the structural basis of the interaction between WT1 and its inhibitors provides valuable insights into the molecular underpinnings of gene expression regulation. As the field of molecular biology continues to evolve, WT1 inhibitors remain a pivotal tool for dissecting the complex interplay between transcription factors and gene networks, opening doors to a deeper comprehension of cellular dynamics.
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
1-β-D-Arabinofuranosylcytosine | 147-94-4 | sc-201628 sc-201628A sc-201628B sc-201628C sc-201628D | 1 g 5 g 25 g 100 g 250 g | $150.00 $263.00 $518.00 $731.00 $1461.00 | 1 | |
Nucleoside analog that disrupts DNA replication and repair by inhibiting DNA polymerase, leading to cell cycle arrest. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $63.00 $158.00 $326.00 | 233 | |
mTOR inhibitor that interferes with cell growth and proliferation signaling pathways, reducing WT1 expression. | ||||||
Belinostat | 414864-00-9 | sc-269851 sc-269851A | 10 mg 100 mg | $156.00 $572.00 | ||
Histone deacetylase inhibitor, modulating gene expression by altering chromatin structure and transcriptional activity. | ||||||
Panobinostat | 404950-80-7 | sc-208148 | 10 mg | $200.00 | 9 | |
Another histone deacetylase inhibitor, inducing changes in gene expression patterns through epigenetic regulation. | ||||||
BI6727 | 755038-65-4 | sc-364432 sc-364432A sc-364432B sc-364432C sc-364432D | 5 mg 50 mg 100 mg 500 mg 1 g | $150.00 $1050.00 $1665.00 $3329.00 $4382.00 | 1 | |
Inhibits Aurora kinase A, leading to cell cycle arrest and disruption of mitotic progression, impacting WT1 expression. | ||||||